American Journal of Medicine and Medical Sciences 2022, 12(2): 126-128
DOI: 10.5923/j.ajmms.20221202.12
Ways to Improve the Surgical Treatment of Obstructive
Ureterohydronephrosis in Children
Atakulov Zhamshed Ostonokulovich
1
, Yusupov Shukhrat Abdurasulovich
2
,
Rakhmatov Bekzod Nasretdinovich
3
, Rakhimov Fakhridin Eshmamatovich
4
,
Abbosov Hozhimuhammad Khabibullaevich
5
1
Doctor of Medical Sciences, Professor of the Department of Pediatric Surgery, Samarkand State Medical Institute
2
Doctor of Medical Sciences, Professor, Head of the Department of Pediatric Surgery No. 1 of the Samarkand State Medical Institute
3
Assistant of the Department of Pediatric Surgery No. 1, Samarkand State Medical Institute
4
Senior Lecturer of the Department of Pediatric Surgery No. 1 of the Samarkand State Medical Institute
5
Resident of the Magistracy of the Department of Pediatric Surgery No. 1, Samarkand State Medical Institute
Abstract
Hydronephrosis and ureterohydronephrosis. A pathological condition associated with the transformation of the
kidney, the expansion of the ureter and the development of malnutrition or atrophy of the parenchyma of the kidney against
the background of a violation of the outflow of urine and its blood supply. According to statistics, ureterohydronephrosis is
quite common. In childhood, it is recorded mainly in boys, more often on the left - a bilateral lesion is diagnosed in 15% of
cases.
Keywords
Ureterohydronephrosis, Kidney, Ureter, Bilateral lesion, Symptoms, Causes of disease
1. Introduction
First of all, let's pay attention
to the spelling of the
diagnosis: Internet sources often confuse (or even use as
synonyms) the concepts of "urethra" and "ureter". Leaving
this on the conscience of the authors, nevertheless, we will
clarify: the urethra is the final (distal, remote) section of the
urinary tract, the urethra itself. The ureter is the ureter, a thin
"hose" of connective tissue through which the fluid (urine)
used after filtering the blood flows from the kidney to the
bladder. Since the right kidney is located slightly lower than
the left, the right ureter is also normally a few centimeters
shorter; in addition, due to anatomical differences, the
ureters are shorter in women. In general, their length in
adults varies between 22-30 cm,
while the thickness in
different areas is different and amounts to 3-10 mm.
And between the ages of 20 and 40, the disease occurs in
1% of people. Women suffer twice as often as men, which
is associated with pregnancy and the prevalence of tumor
gynecological pathology.
Further,
hydronephrosis,
or
hydronephrotic
transformation, is a pathological condition of the kidney, in
which its cavities are mechanically expanded from the inside
by excess fluid pressure on the walls. This pathology is
considered to be quite common, although there are
apparently no exact statistical data in terms of the proportion
Received: Jan. 25, 2022; Accepted: Feb. 11, 2022; Published: Feb. 15, 2022
Published online at http://journal.sapub.org/ajmms
of the healthy population: the spread of published estimates
is too large. It is known, however, that in the volume of all
officially diagnosed nephropathologist, the proportion of
hydronephrosis is approximately 5%, and among the causes
of hospitalization in nephrological and urological hospitals -
about 2%.
It is important to note that hydronephrosis is not a
harmless anatomical anomaly: chronically elevated pressure
of excess fluid not only stretches the pelvicalyceal system of
the kidney, but also inevitably disrupts its performance.
Under such conditions, nephrons (single
cells of the renal
parenchyma - functional, filtering tissue) receive insufficient
nutrition, their dystrophy begins and progresses, and then
atrophy - complete functional failure of specialized cells,
massive "failure" and death, reduction of parenchymal
tissue in volume. The quantitative proportion between
functioning and atrophied nephrons largely determines the
clinical picture, prognosis, and
therapeutic strategy for
hydronephrosis. The cause of ureterohydronephrosis is a
violation of the laying in the embryonic period of the organs
of the urinary system at the level of the ureter-bladder.
A
sharp
violation
of
urodynamics
in
ureterohydronephrosis that occurs in the prenatal period
rapidly leads to impaired kidney function, and in a bilateral
process, in the absence of a timely and high-quality operation,
leads to renal failure. Early diagnosis and treatment
according to indications is the key to success in this type of
pathology.
American Journal of Medicine and Medical Sciences 2022, 12(2): 126-128
127
Finally, the prefix "uretero-" to this diagnosis means that
under the influence of the pathological distribution of
pressures, not only the renal structures proper, but also the
corresponding ureter expand. It is easy to see that this
situation is more complex and severe compared to "simple"
hydronephrosis, often requiring more radical intervention.
Ureterohydronephrosis is a pathological expansion of the
pelvis and calyces of the kidneys, as well as the ureter. It
develops in violation of the natural outflow of urine.
Pathology is dangerous because
it leads to the death of
kidney cells and causes acute renal failure. Therefore, it is
very important to consult a doctor in a timely manner for the
diagnosis and treatment of ureterohydronephrosis.
In pediatric practice, megaureter is one of the diseases that
lead to impaired renal function, moreover, in a bilateral
process, up to renal failure. With the expansion of the ureter,
its transport function suffers and it becomes impossible to
quickly move urine into the bladder and remove the
microbial flora penetrating the urinary tract, causing chronic
inflammation of the kidneys (pyelonephritis). Another
dangerous consequence of the
stagnation of urine in the
ureter is an increase in pressure in the renal pelvis and
calyces, which causes impaired renal circulation. The
outcome of chronic inflammation and impaired renal
circulation is scarring of the renal tissue (parenchyma) with
loss of function (secondary wrinkling of the kidney,
nephrosclerosis).
What are the causes of megaureter? There are several
reasons for the formation of a megaureter. The main reason
is increased pressure inside the ureter with difficulty in the
outflow of urine. And sometimes the pressure is normalized,
and the expansion of the ureter remains. There is also
congenital insufficiency of the muscular membrane of the
ureter. In this case, the normal muscle layer of the ureter is
replaced by scar inelastic tissue. The ureter is so weak that it
is unable to effectively push urine into the bladder. Another
cause of a megaureter is a narrowing of the ureter at its
junction with the bladder. High-grade vesicoureteral reflux
(VUR - reflux of urine from the bladder into the ureter and
kidney) can also be the cause
of the development of a
megaureter. Bilateral megaureter is more often the result of a
violation of the outflow of urine through the urethra, due to
the presence of a congenital valve in the urethra or persistent
spasm of the urethral sphincter, which occurs in neurological
disorders. Such a megaureter is called secondary.
How is megaureter manifested? Megaureter is usually
diagnosed by fetal ultrasound. After birth, in the absence of
pathology of the bladder and urethra, the megaureter usually
does not manifest itself clinically. In the future, if the
diagnosis was not made in utero, the disease may manifest
itself as an unexpected attack of pyelonephritis. Older
children sometimes complain of pain in the abdomen or in
the lumbar region, an admixture of blood in the urine, There
are 2 main forms of the disease - acute and chronic.
Acute symptoms are:
pain in the lower abdomen;
frequent urge to urinate (mainly at night);
high blood pressure;
renal colic.
The patient may notice reddening of the urine due to the
appearance of blood impurities in it. Also, patients complain
of weakness and general malaise, as well as lack of appetite.
In
the chronic form, it may be asymptomatic for several
years.
Diagnosing ureterohydronephrosis is quite difficult
because of the pronounced symptoms that are characteristic
of this particular disease.
The first time the presence of a megaureter is usually
reported by a specialist in ultrasound diagnostics. If a
megaureter is found in a child with ultrasound, it is necessary
to prepare for a complete urological examination to
determine the cause, prognosis and treatment tactics.
Intravenous (excretory) urography allows you to see the
anatomical structure of the ureters, to determine how well the
kidneys produce urine and are released from it. On urograms,
the diameter of the ureters can be seen, which, with a
megaureter, is more than 7-10 mm.
Voiding cystourethrography (VCUG) is performed if
vesicoureteral reflux is suspected (reflux
of urine from the
bladder into the ureter), to determine the patency of the
urethra, exclude vesicoureteral reflux, and indirectly assess
bladder function.
Radioisotope examination of the kidneys (static or
dynamic nephroscintigraphy) - is performed to assess the
function of the kidneys and the degree of violation of the
outflow of urine through the affected ureter.
Ureterohydronephrosis is a pathological expansion of the
pelvis and calyces of the kidneys, as well as the ureter.
It develops in violation of the natural outflow of urine.
Pathology is dangerous because it leads to the death of
kidney cells and causes acute renal failure.
Children operated on by the method of urethrocystone
anastomosis, in the immediate postoperative period,
complained of an intermittent stream of urine, discomfort at
the end of urination, pain at the end of urination, a feeling of
urge to urinate after the act of micturition,
as well as pain
during urination. These clinic was associated with the
condition after the operation of ureterocystone anastomosis
(bladder injury, urethral catheterization, urinary infection
and exacerbation of chronic cystitis); after appropriate
treatment, the above symptoms ceased.